Finding My Way-UK: Promoting Positive Psychological Outcomes in People Living With and Beyond Curatively Treated Cancer

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age16+
SponsorEdge Hill University

About this trial

The goal of this pilot randomised trial is to evaluate whether an online psychosocial intervention (Finding My Way-UK) is feasible and acceptable for individuals living with and beyond curatively treated cancer. The main questions it aims to answer are:

1. Is Finding My Way-UK feasible and acceptable for individuals living with and beyond curatively treated cancer? 2. Are there preliminary signals of efficacy in benefit finding and other well-being outcomes (hope, resilience, and subjective well-being)? 3. What is the potential role of information-seeking styles and self-management self-efficacy?

Participants will be randomly assigned to one of two groups:

1. Finding My Way-UK Intervention group: access a four-week, self-guided online program with six modules covering coping with treatment side effects, managing emotions, social support, body image, and post-treatment adjustment. 2. Control group: receive a digital information pack listing national psychological support resources.

All study activities will take place online. Participants will complete questionnaires before the program, after four weeks, and three months later.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Diagnosed with any cancer within the past 12 months;

Cancer is being (or, indeed, was) treated with curative intent;

Aged 16 years or older;

Possess sufficient English proficiency to provide informed consent and use the program;

Disqualifiers

Diagnosis of cancer not being treated with curative intent (for example, metastatic, stage IV, or otherwise advanced-stage disease);

And/Or have a severe comorbidity that may hinder their ability to participate fully (such as being unable to complete study procedures or provide informed consent).

Trial design

Design model

Parallel

Treatments tested in this trial

  • Finding My Way-UK

    Behavioral

    Self-guided, web-based psychosocial intervention integrating cognitive-behavioural, psychoeducational, and mindfulness-based strategies to support people living with and beyond curatively treated cancer. Six modules delivered online; participants complete flexibly over four weeks.

  • Treatment-As-Usual Control

    Other intervention

    Digital information pack (PDF) signposting to existing UK cancer-support organisations and psychological resources. Distributed by email; no structured therapeutic program or study-specific content.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Finding My Way-UK InterventionExperimental treatment 1 intervention
Group B: Control - Information PackOther 1 intervention

Trial outcomes

Primary outcomes

1

Recruitment Rate

The feasibility of recruitment will be assessed by the number of participants enrolled in the study per month.

Time frame
From enrolment of the first participant until the recruitment target is reached (up to 6 months)
2

Intervention Adherence: Modules Accessed

The level of engagement with the Finding My Way-UK program, defined as the number of intervention modules accessed (opened) by each participant on the Finding My Way-UK platform.

Time frame
At post-intervention (week 4)
3

Intervention Adherence: Modules Completed

The number of intervention modules completed by each participant on the Finding My Way-UK platform.

Time frame
At post-intervention (week 4)
4

Retention Rate at Post-Intervention

Assessed by the percentage of participants who complete the post-intervention outcome assessment.

Time frame
At post-intervention (week 4)

Secondary outcomes

1

Change from Baseline in Benefit Finding Score

Measured using the Benefit Finding Scale (BFS). The BFS contains 17 items rated from 1 = not at all to 5 = extremely, summed to a total score range of 17-85, with higher scores indicating greater benefit finding. Analyses will be descriptive and exploratory, focusing on estimating pre-post effect sizes and the proportion of participants showing reliable improvement using Reliable Change Indices; no formal hypothesis testing will be performed.

Time frame
Baseline (pre-intervention), post-intervention (week 4), and 3 months post-intervention
2

Change from Baseline in Satisfaction with Life

Subjective well-being will be assessed with the Satisfaction with Life Scale (SWLS). The SWLS comprises 5 items rated from 1 = strongly disagree to 7 = strongly agree, summed to give a total score range of 5-35, where higher scores reflect greater life satisfaction.

Time frame
Baseline (pre-intervention), post-intervention (week 4), and 3 months post-intervention
3

Change from Baseline in Hope

Measured using the Herth Hope Index (HHI). The HHI includes 12 items rated 1 = strongly disagree to 4 = strongly agree, summed for a total score range of 12-48; higher values indicate greater hope.

Time frame
Baseline (pre-intervention), post-intervention (week 4), and 3 months post-intervention
4

Change from Baseline in Resilience

Measured using the Connor-Davidson Resilience Scale-10 (CD-RISC-10). Ten items rated 0 (not true at all) to 4 (true nearly all the time) yield a total score range of 0-40, with higher scores indicating greater resilience.

Time frame
Baseline (pre-intervention), post-intervention (week 4), and 3 months post-intervention

Other outcomes

1

Change from Baseline in Self-Management Self-Efficacy

Measured using the Self-Efficacy for Managing Chronic Disease Scale. Six items rated 1-10; mean score represents overall self-efficacy (higher scores indicate higher self-management self-efficacy).

Time frame
Baseline (pre-intervention), post-intervention (week 4), and 3 months post-intervention
2

Information-Seeking Style

Assessed using the Cancer Information-Seeking Preferences Questionnaire, a single-item measure that classifies participants into one of five information-seeking styles: intense seekers, complementary seekers, fortuitous seekers, minimal/uninterested seekers, or guarded avoiders.

Time frame
At baseline (pre-intervention)

Sponsors and contacts

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Edge Hill University

Lead sponsor

Flinders University

Collaborator

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